CN113528879A - Polycrystalline diamond combined by compounds generated by in-situ reaction and preparation method thereof - Google Patents
Polycrystalline diamond combined by compounds generated by in-situ reaction and preparation method thereof Download PDFInfo
- Publication number
- CN113528879A CN113528879A CN202110805725.8A CN202110805725A CN113528879A CN 113528879 A CN113528879 A CN 113528879A CN 202110805725 A CN202110805725 A CN 202110805725A CN 113528879 A CN113528879 A CN 113528879A
- Authority
- CN
- China
- Prior art keywords
- diamond
- temperature
- pressure
- powder
- ball milling
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C1/00—Making non-ferrous alloys
- C22C1/04—Making non-ferrous alloys by powder metallurgy
- C22C1/05—Mixtures of metal powder with non-metallic powder
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/10—Sintering only
- B22F3/1039—Sintering only by reaction
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C26/00—Alloys containing diamond or cubic or wurtzitic boron nitride, fullerenes or carbon nanotubes
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Manufacturing & Machinery (AREA)
- Carbon And Carbon Compounds (AREA)
- Ceramic Products (AREA)
- Powder Metallurgy (AREA)
Abstract
The invention provides a polycrystalline diamond combined by compounds generated by an in-situ reaction and a preparation method thereof, belonging to the technical field of superhard composite materials. The method comprises the steps of performing ball milling on Ti powder, Si powder and nano-diamond to perform mechanical alloying to obtain a bonding agent material; the molar ratio of the Ti powder to the Si powder is equal to 3; the molar ratio of the nano diamond to the Si powder is more than 2 and less than or equal to 5; and mixing the bonding agent with the micron diamond, prepressing the obtained mixture, and sintering the obtained prepressed blank at high temperature and high pressure to obtain the polycrystalline diamond combined with the compound generated by the in-situ reaction. Due to the excessive addition of the nano-diamond and the high-pressure environment, the nano-diamond is left after reacting with Ti and Si and can be remained, and the problem that the addition of Si, Ti, B, Ni and the like in the traditional PCD preparation method is easy to leave unreacted and complete Ti, Si and compounds thereof in a shed frame area far away from the diamond so as to leave soft spots is solved.
Description
Technical Field
The invention relates to the technical field of superhard composite materials, in particular to polycrystalline diamond combined with a compound generated by an in-situ reaction and a preparation method thereof.
Background
Diamond is currently the hardest material known in the world. Since the 50 s of the last century, diamond and its products have been widely used in the machining field as cutting, drilling or polishing tools. However, synthetic diamond is not easy to be directly used as a cutting tool because its particles are fine (the particle size of industrial diamond is generally less than 1mm), and usually diamond fine powder (0.5 to 60 μm) is used as a main body, and sintered together by adding a binder powder or by a fusion-precipitation reaction to obtain an isotropic polycrystalline diamond sintered body, namely PCD.
Conventional PCD materials fall into two main categories: binders of the Ti-Si series sinter PCD and PCD sintered by the cobalt-based metallic sweep reaction. The Ti-Si series of PCD is formed by sintering Ti powder, Si powder and diamond micro powder under the conditions of high temperature and high pressure, and connecting diamond by covalent bond compounds TiC and SiC formed in the sintering process. In some cases, a small amount of boron, nickel or the like is added to improve sinterability or sintered body properties. Because of solid state sintering, Ti, Si and the like form TiSi compounds at the position far away from the surface of the micron diamond, even single substances of Ti and Si are remained; the micro-diamonds are contacted with each other to leave a diamond-free area to form a 'shed frame area', so that the uniformity of the PCD hardness is reduced; and the strength of the material of the 'shed frame area' is low, cracks are often developed from the material, so that the toughness of the PCD material is poor, and brittle fracture is easy to occur. The swept-growth type PCD mainly based on Co has the characteristics of easy sintering and high toughness, however, the residual Co greatly weakens the service performance of the PCD, and particularly, catalyst metals such as Co and the like can promote the transformation of diamond to graphite under the conditions of normal pressure and high temperature. Since the thermal expansion coefficient of metal is much higher than that of diamond, stress concentration is easy to generate during the use process, and cracks are generated.
In recent years, ternary layered compound Ti3SiC2Ceramics have attracted considerable interest to physical and material scientists because of their excellent physicochemical properties. On the one hand, it has good thermal and electrical conductivity similar to that of a metal material, and excellent workability; on the other hand, the ceramic material also has similar physical and chemical properties with the ceramic material, such as high melting point, oxidation resistance, chemical corrosion resistance, high temperature resistance, excellent thermal shock resistance and the like. Ti3SiC2Phase with superhard material, able to overcome the respective disadvantages of metals and ceramics, so Ti3SiC2The unique properties may improve some of the properties of current PCD materials. Recently, there have been many cases where Ti is directly added3SiC2PCD as a binder, however, Ti3SiC2The hardness of the phase is far different from that of diamond and is far lower than that of TiC, SiC and the like. Simple substance materials such as Ti, Si, C and the like are added in the process of preparing PCD, and the reaction is expected to generate Ti in the process of preparing PCD3SiC2In addition, it is desired to increase the bonding strength between diamond and a binder by generating TiC and SiC at a contact portion with the diamond surface. However, due to the different particle sizes and density differences of the added powders of Si, Ti, C, etc., the uniformity of the mixed powder is poor, so that complete reaction cannot be achieved, and elemental materials often remain at the aggregation positions of Ti, Si, C, etc., and are partially concentrated in a "shelf area", so that soft spots exist in the area, and the problem of the "shelf area" cannot be solved.
Disclosure of Invention
The invention aims to provide a polycrystalline diamond combined by compounds generated by in-situ reaction and a preparation method thereof, and solves the problem that Si, Ti, B, Ni and the like added in the traditional PCD preparation method are easy to leave unreacted Ti, Si and compounds thereof in a shed frame area of the diamond so as to leave soft spots.
In order to achieve the above object, the present invention provides the following technical solutions:
the invention provides a preparation method of polycrystalline diamond combined by compounds generated by in-situ reaction, which is characterized by comprising the following steps:
carrying out ball milling on Ti powder, Si powder and nano diamond, and carrying out mechanical alloying to obtain a bonding agent material; the molar ratio of the Ti powder to the Si powder is equal to 3; the molar ratio of the nano diamond to the Si powder is more than 2 and less than or equal to 5;
mixing the bonding agent material with the micron diamond to obtain a mixture;
prepressing the mixture to obtain a prepressing blank;
sintering the pre-pressed blank at high temperature and high pressure to obtain polycrystalline diamond combined with a compound generated by an in-situ reaction;
the high-temperature high-pressure sintering comprises the following steps: sequentially carrying out first high-temperature high-pressure sintering and second high-temperature high-pressure sintering; the temperature of the first high-temperature high-pressure sintering is 1100-1300 ℃, and the heat preservation time is 5-15 min; the temperature of the second high-temperature high-pressure sintering is 1350-1500 ℃, and the heat preservation time is 5-40 min;
the pressure of the first high-temperature high-pressure sintering and the second high-temperature high-pressure sintering is independently more than 5.5 GPa.
Preferably, the particle diameters of the Ti powder and the Si powder are independently 3-10 μm.
Preferably, the particle size of the nano-diamond is 2-100 nm.
Preferably, the ball-milling ball-material ratio is 20: 1; the rotating speed of the ball milling is 350-450 r/min; the ball milling time is more than 120 min.
Preferably, the particle size of the micro diamond is 0.5-40 μm.
Preferably, the mass content of the binding agent in the mixture is 10-40%.
Preferably, the pre-pressing pressure is 100-200 MPa.
Preferably, the dwell time of the pre-pressing is above 10 min.
The invention provides a polycrystalline diamond prepared by the preparation method in the scheme, which comprises micron diamond, nano diamond, TiC and Ti3SiC2SiC and TiSi phases.
Preferably, the TiSi phase comprises TiSi2Phase and/or Ti5Si3And (4) phase(s).
The invention provides a preparation method of polycrystalline diamond combined by compounds generated by in-situ reaction, which comprises the following steps: carrying out ball milling on Ti powder, Si powder and nano diamond, and carrying out mechanical alloying to obtain a bonding agent material; the molar ratio of the Ti powder to the Si powder is equal to 3; the molar ratio of the nano diamond to the Si powder is more than 2 and less than or equal to 5; mixing the bonding agent material with the micron diamond to obtain a mixture; prepressing the mixture to obtain a prepressing blank; sintering the pre-pressed blank at high temperature and high pressure to obtain polycrystalline diamond combined with a compound generated by an in-situ reaction; the high-temperature high-pressure sintering comprises sequentially carrying out first high-temperature high-pressure sintering and second high-temperature high-pressure sintering; the temperature of the first high-temperature high-pressure sintering is 1100-1300 ℃, and the heat preservation time is 5-15 min; the temperature of the second high-temperature high-pressure sintering is 1350-1500 ℃, and the heat preservation time is 5-40 min; the pressure of the first high-temperature high-pressure sintering and the second high-temperature high-pressure sintering is independently more than 5.5 GPa.
According to the invention, the Ti powder, the Si powder and the nano diamond are subjected to ball milling, so that each powder is uniformly refined and is forced to be subjected to mechanical alloying, the powder is in full contact, the surface of the refined powder particles is fresh, the specific surface area is increased, the reaction in the sintering process is in full favor, and a guarantee is provided for avoiding residual simple substance Ti and Si; the in situ reaction in this application is carried out in two stages: in the first high-temperature high-pressure sintering stage, Ti-Si-nano diamond reacts to generate Ti3SiC2And a small amount of TiC and SiC, and because the nano-diamond is excessively added, the residual simple substances of Ti and Si after the reaction is avoided, meanwhile, part of the nano-diamond is remained and retained in a diamond structure, and the equation of the reaction in the first high-temperature high-pressure sintering stage is as follows: 3Ti + Si +2C → Ti3SiC2；Ti+C→TiC；Si+C→SiC. In the second high-temperature high-pressure sintering stage, the compound Ti generated in the first stage3SiC2Most of the decomposition occurs to form second stage compounds TiC and SiC and a small amount of TiSi phase; the equation for the reaction is as follows: ti3SiC2→TiC+SiC+TiSi。
Due to the excessive addition of the nano-diamond and a high-pressure environment, the nano-diamond is remained after the reaction with Ti and Si and can be remained in a diamond structure. The remained nano-diamond is distributed at any part of a reaction product, so that the hardness of the parts is improved due to the existence of the remained nano-diamond, and the problem that the Ti, the Si and the compound thereof which are not completely reacted are easy to remain in a 'shelf area' far away from the diamond by adding Si, Ti, B, Ni and the like in the traditional PCD preparation method is solved, thereby leaving soft spots. The rest of the nano-diamond can also be used as an abrasive.
In addition, a small amount of Ti can be retained under high temperature and high pressure conditions3SiC2The toughness of the PCD is improved; a small amount of Ti3SiC2Also has self-lubricating effect.
The formation and decomposition processes of the two stages enable the grain size of the compound to be finer and finer, and the strength and the toughness of the PCD can be improved.
Drawings
Fig. 1 is an SEM image of polycrystalline diamond prepared according to example 5;
FIG. 2 is an enlarged view of a portion of FIG. 1;
fig. 3 is an XRD pattern of polycrystalline diamond prepared in example 5, example 9, and example 2;
fig. 4 is an XRD pattern of polycrystalline diamond prepared in examples 6, 7, 8 and 10.
Detailed Description
The invention provides a preparation method of polycrystalline diamond combined by compounds generated by in-situ reaction, which comprises the following steps:
carrying out ball milling on Ti powder, Si powder and nano diamond, and carrying out mechanical alloying to obtain a bonding agent material; the molar ratio of the Ti powder to the Si powder is equal to 3; the molar ratio of the nano diamond to the Si powder is more than 2 and less than or equal to 5;
mixing the bonding agent material with the micron diamond to obtain a mixture;
prepressing the mixture to obtain a prepressing blank;
sintering the pre-pressed blank at high temperature and high pressure to obtain polycrystalline diamond combined with a compound generated by an in-situ reaction;
the high-temperature high-pressure sintering comprises sequentially carrying out first high-temperature high-pressure sintering and second high-temperature high-pressure sintering; the temperature of the first high-temperature high-pressure sintering is 1100-1300 ℃, and the heat preservation time is 5-15 min; the temperature of the second high-temperature high-pressure sintering is 1350-1500 ℃, and the heat preservation time is 5-40 min;
the pressure of the first high-temperature high-pressure sintering and the second high-temperature high-pressure sintering is independently more than 5.5 GPa.
In the present invention, the starting materials used are all commercially available products well known in the art, unless otherwise specified.
The invention carries out ball milling on Ti powder, Si powder and nano diamond, and mechanical alloying is carried out to obtain the bonding agent.
In the present invention, the particle diameters of the Ti powder and the Si powder are independently preferably 3 to 10 μm, more preferably 5 to 8 μm, and still more preferably 6 to 7 μm.
In the present invention, the particle size of the nanodiamond is preferably 2 to 100nm, and more preferably 2 to 12nm or 100 nm.
In the invention, the molar ratio of the Ti powder to the Si powder is equal to 3; the molar ratio of the nano diamond to the Si powder is more than 2 and less than or equal to 5, preferably 3-5, and more preferably 3.5-4.5. According to the invention, the molar ratio of the Ti powder, the Si powder and the nano-diamond is controlled within the range, so that the nano-diamond is excessive, and partial nano-diamond is ensured to be remained.
In the present invention, the ball-to-material ratio of the ball mill is preferably 20: 1; the rotation speed of the ball milling is preferably 350-450 r/min, and more preferably 400 r/min; the time for ball milling is preferably 120min or more, more preferably 120 min. The invention preferably adopts a planetary ball mill for ball milling.
According to the invention, the Ti powder, the Si powder and the nano diamond are subjected to ball milling, so that each powder is uniformly refined and is forced to be subjected to mechanical alloying, the powder is in full contact, the surface of the refined powder particles is fresh, the specific surface area is increased, the reaction in the sintering process is in full favor, and a guarantee is provided for avoiding residual simple substance Ti and Si.
After the bonding agent material is obtained, the bonding agent material is mixed with the micron diamond to obtain a mixture.
In the present invention, the particle size of the micro diamond is preferably 0.5 to 40 μm, more preferably 5 to 35 μm, and further preferably 10 to 30 μm.
The invention has no special requirements on the mixing process, can uniformly mix all materials, and can adopt ball milling specifically. In the invention, the mass content of the binding agent in the mixture is preferably 10-40%, more preferably 15-35%, and even more preferably 20-30%.
After the mixture is obtained, the invention carries out prepressing on the mixture to obtain a prepressing blank. In the invention, the pre-pressing pressure is preferably 100-200 MPa, more preferably 120-180 MPa, and further preferably 130-160 MPa; the time for the pre-pressing is preferably 10min or more, more preferably 10 min. The invention preferably performs the pre-pressing in a hydraulic press. The invention makes the prepressing blank as compact as possible by prepressing, which is beneficial to high-temperature and high-pressure sintering.
After the pre-pressed blank is obtained, the pre-pressed blank is sintered at high temperature and high pressure to obtain the polycrystalline diamond combined by the compound generated by the in-situ reaction.
In the present invention, the high-temperature high-pressure sintering includes: sequentially carrying out first high-temperature high-pressure sintering and second high-temperature high-pressure sintering; the temperature of the first high-temperature high-pressure sintering is 1100-1300 ℃, and the heat preservation time is 5-15 min; the temperature of the second high-temperature high-pressure sintering is 1350-1500 ℃, and the heat preservation time is 5-40 min.
Preferably, the temperature of the first high-temperature high-pressure sintering is preferably 1150-1250 ℃, and the heat preservation time is preferably 10 min; the temperature of the second high-temperature high-pressure sintering is preferably 1400-1450 ℃, and the heat preservation time is preferably 10-30 min.
In the present invention, the first high-temperature high-pressure sintering and the second high-temperature high-pressure sintering are independently performed at a pressure of 5.5GPa or more, and more preferably 5.5 to 7.0 GPa. In the present invention, the pressure of the first high temperature and high pressure sintering and the second high temperature and high pressure sintering is preferably the same.
The pre-pressed blank is preferably assembled with a pressure transmission medium, a carbon tube for heating, a conductive steel ring, a graphite gasket and the like into an assembly according to the requirements of high-temperature and high-pressure sintering, and then the assembly is placed on an anvil of a high-pressure press for high-temperature and high-pressure sintering. The present invention does not require any special assembly process, as is well known in the art.
Preferably, the pressure is increased to the pressure of the first high-temperature high-pressure sintering within 10-20 min, then the temperature is increased to the temperature of the first high-temperature high-pressure sintering at the temperature increase rate of 10-100 ℃/min, and the temperature is kept for 5-15 min; and continuously heating from the first high-temperature high-pressure sintering temperature to the second high-temperature high-pressure sintering temperature, keeping the target pressure and the target temperature for 5-40 min, then synchronously reducing the temperature and the pressure to be lower than 60 ℃ and atmospheric pressure, stopping the machine, taking out the assembly to obtain a polycrystalline diamond blank, and polishing to obtain the polycrystalline diamond with a compact structure.
In the first high-temperature high-pressure sintering stage, the Ti-Si-nano diamond reacts to form Ti3SiC2And a small amount of TiC and SiC, and because the nano-diamond is excessively added, the residual simple substances of Ti and Si after the reaction is avoided, and meanwhile, part of the nano-diamond remains, namely Ti3SiC2Is the main compound of the first high-temperature high-pressure sintering stage; the equation for the reaction is:
3Ti+Si+2C→Ti3SiC2；
Ti+C→TiC；
Si+C→SiC。
in the second high-temperature high-pressure sintering stage, the compound Ti generated in the first stage3SiC2Most of the decomposition occurs to form second stage compounds TiC and SiC and a small amount of TiSi phase; the equation for the reaction is as follows:
Ti3SiC2→TiC+SiC+TiSi。
due to the excessive addition of the nano-diamond and the high-pressure environment, the nano-diamond is left after reacting with Ti and Si and can be remained. The remained nano-diamond is distributed at any part of a reaction product, so that the hardness of the parts is improved due to the existence of the remained nano-diamond, and the problem that the Ti, the Si and the compound thereof which are not completely reacted are easy to remain in a 'shelf area' far away from the diamond by adding Si, Ti, B, Ni and the like in the traditional PCD preparation method is solved, thereby leaving soft spots. The rest of the nano-diamond can also be used as an abrasive.
The invention provides a polycrystalline diamond prepared by the preparation method in the scheme, which comprises micron diamond, nano diamond, TiC and Ti3SiC2SiC and TiSi phases. The TiSi phase preferably comprises TiSi2Phase and/or Ti5Si3And (4) phase(s). The nano-diamond is distributed in a shelf area of the polycrystalline diamond, so that soft points Ti left by the polycrystalline diamond are avoided3SiC2The presence of the phase improves the toughness of the PCD, while also having a self-lubricating effect.
The in-situ reaction-generating compound-bonded polycrystalline diamond and the method for preparing the same according to the present invention will be described in detail with reference to the following examples, which should not be construed as limiting the scope of the present invention.
The particle size of Ti powder used in the following examples is 3 to 10 μm, and the particle size of Si powder used is 3 to 10 μm.
Example 1
(1) 35g of bonding agent, wherein the molar ratio of Ti to Si to the nano-diamond is 3:1:3 (the mass ratio of the nano-diamond particle size is 20% of 2-12 nm, and the particle size is 80% of 100 nm); 65g of micro diamond (wherein the grain diameter is 10 microns 35g, 6 microns 20g, 0.5 microns 10 g); firstly, mixing weighed titanium powder, silicon powder and nano-diamond, filling the mixture into a ball milling tank under the argon condition of a glove box, and sealing the ball milling tank; taking out and putting into a planetary ball mill, wherein the ball-to-material ratio is 20:1, mechanically mixing at 350r/min for 120min, and carrying out mechanical alloying to prepare a bonding agent; taking down the ball milling tank after stopping the machine, opening the ball milling tank under the argon condition of a glove box, putting the weighed micron diamond, uniformly scraping and stirring the micron diamond and the bonding agent, and mechanically ball milling and mixing the mixture for 20min to prepare a mixture; taking down the ball milling tank after stopping the machine, opening the ball milling tank under the argon condition of the glove box, and taking out the prepared mixture for later use;
(2) taking out the mixture, weighing according to the requirement, filling the mixture into a Ti tube, and plugging two ends of the Ti tube; putting the mixture into a metal die, and prepressing and molding the mixture in a hydraulic press at the pressure of 100MPa and room temperature to prepare a prepressed blank;
(3) assembling the pre-pressed blank with pressure-transmitting medium, heating carbon tube, conducting steel ring, graphite gasket, etc. to form the assembly, and setting the assembly in the anvil position of cubic apparatus press while applying high temperature and high pressure. The high-temperature high-pressure process flow comprises the following steps: firstly, increasing the pressure to 6GPa within 20min, then increasing the temperature to 1250 ℃ at the temperature increase rate of 20 ℃/min, and keeping the temperature for 10min under the target pressure and temperature; and then continuously heating to 1350 ℃, keeping the temperature and the pressure for 30min, synchronously reducing the temperature and the pressure to 60 ℃ and atmospheric environment pressure, stopping the machine, taking out the assembly to obtain a polycrystalline diamond blank, and polishing to obtain the polycrystalline diamond with a compact structure.
Example 2
(1) 40g of bonding agent, namely Ti, Si and nano-diamond in a molar ratio of 3:1:5 (wherein the nano-diamond has a particle size of 2-12 nanometers accounting for 40% by mass and a particle size of 100 nanometers accounting for 60%), 60g of micro-diamond (wherein the particle size is 10 micrometers and 35g, 6 micrometers and 20g, and 0.5 micrometers and 5 g); firstly, mixing weighed titanium powder, silicon powder and nano-diamond, filling the mixture into a ball milling tank under the argon condition of a glove box, and sealing the ball milling tank; taking out and putting into a planetary ball mill, wherein the ball-to-material ratio is 20:1, mechanically mixing at 350r/min for 120min, and carrying out mechanical alloying to prepare a bonding agent; taking down the ball milling tank after stopping the machine, opening the ball milling tank under the argon condition of a glove box, putting the weighed micron diamond, uniformly scraping and stirring the micron diamond and the bonding agent, and mechanically ball milling and mixing the mixture for 20min to prepare a mixture; taking down the ball milling tank after stopping the machine, opening the ball milling tank under the argon condition of the glove box, and taking out the prepared mixture for later use;
(2) taking out the mixture, weighing according to the requirement, filling the mixture into a Ti tube, and plugging two ends of the Ti tube; putting the mixture into a metal die, and prepressing and molding the mixture in a hydraulic press at the pressure of 200MPa and room temperature to prepare a prepressed blank;
(3) the pre-pressing blank is assembled with a pressure transmission medium, a carbon tube for heating, a conductive steel ring, a graphite gasket and the like into an assembly according to a common preparation method of the polycrystalline diamond, and the assembly is placed at the anvil position of a cubic press and is applied with high temperature and high pressure. The high-temperature high-pressure process flow comprises the following steps: firstly, increasing the pressure to 7GPa within 20min, then increasing the temperature to 1150 ℃ at the temperature increase rate of 10 ℃/min, and keeping the temperature for 10min under the target pressure and temperature; and then continuously heating to 1400 ℃, keeping the temperature and the pressure for 15min, synchronously reducing the temperature and the pressure to 60 ℃ and atmospheric environment pressure, stopping the machine, taking out the assembly to obtain a polycrystalline diamond blank, and polishing to obtain the polycrystalline diamond with a compact structure.
Example 3
(1) 10g of bonding agent, namely, 90g of micro-diamond (the grain diameter of the nano-diamond is 100 nanometers, 40g of grain diameter of the micro-diamond is 40 micrometers, 25g of grain diameter of the micro-diamond is 25 micrometers, 15g of grain diameter of the micro-diamond is 10g of grain diameter of the micro-diamond is 6 micrometers) according to the molar ratio of Ti to Si to the nano-diamond being 3:1: 5; firstly, mixing weighed titanium powder, silicon powder and nano-diamond, filling the mixture into a ball milling tank under the argon condition of a glove box, and sealing the ball milling tank; taking out and putting into a planetary ball mill, wherein the ball-to-material ratio is 20:1, mechanically mixing at 350r/min for 120min, and carrying out mechanical alloying to prepare a bonding agent; taking down the ball milling tank after stopping the machine, opening the ball milling tank under the argon condition of a glove box, putting the weighed micron diamond, uniformly scraping and stirring the micron diamond and the bonding agent, and mechanically ball milling and mixing the mixture for 20min to prepare a mixture; taking down the ball milling tank after stopping the machine, opening the ball milling tank under the argon condition of the glove box, and taking out the prepared mixture for later use;
(2) taking out the mixture, weighing according to the requirement, filling the mixture into a Ti tube, and plugging two ends of the Ti tube; putting the mixture into a metal die, and prepressing and molding the mixture in a hydraulic press at the pressure of 100MPa and room temperature to prepare a prepressed blank;
(3) the pre-pressing blank is assembled with a pressure transmission medium, a carbon tube for heating, a conductive steel ring, a graphite gasket and the like into an assembly according to a common preparation method of the polycrystalline diamond, and the assembly is placed at the anvil position of a cubic press and is applied with high temperature and high pressure. The high-temperature high-pressure process flow comprises the following steps: firstly, increasing the pressure to 7GPa within 30min, then increasing the temperature to 1200 ℃ at the temperature increase rate of 10 ℃/min, and keeping the temperature for 10min under the target pressure and temperature; and then continuously heating to 1450 ℃, keeping the temperature and the pressure for 40min, synchronously reducing the temperature and the pressure to 60 ℃ and atmospheric environment pressure, stopping the machine, taking out the assembly to obtain a polycrystalline diamond blank, and polishing to obtain the polycrystalline diamond with a compact structure.
Example 4
(1) 40g of bonding agent, namely Ti, Si and nano-diamond in a molar ratio of 3:1:5 (wherein the nano-diamond has a particle size of 2-12 nanometers accounting for 10% by mass and a particle size of 100 nanometers accounting for 90%), and 60g of micro-diamond (wherein the particle size is 10 micrometers 30g, 6 micrometers 20g, and 0.5 micrometer 10 g); firstly, mixing weighed titanium powder, silicon powder and nano-diamond, filling the mixture into a ball milling tank under the argon condition of a glove box, and sealing the ball milling tank; taking out and putting into a planetary ball mill, wherein the ball-to-material ratio is 20:1, mechanically mixing at 350r/min for 120min, and carrying out mechanical alloying to prepare a bonding agent; taking down the ball milling tank after stopping the machine, opening the ball milling tank under the argon condition of a glove box, putting the weighed micron diamond, uniformly scraping and stirring the micron diamond and the bonding agent, and mechanically ball milling and mixing the mixture for 20min to prepare a mixture; taking down the ball milling tank after stopping the machine, opening the ball milling tank under the argon condition of the glove box, and taking out the prepared mixture for later use;
(2) taking out the mixture, weighing according to the requirement, filling the mixture into a Ti tube, and plugging two ends of the Ti tube; putting the mixture into a metal die, and prepressing and molding the mixture in a hydraulic press at the pressure of 200MPa and room temperature to prepare a prepressed blank;
(3) the pre-pressing blank is assembled with a pressure transmission medium, a carbon tube for heating, a conductive steel ring, a graphite gasket and the like into an assembly according to a common preparation method of the polycrystalline diamond, and the assembly is placed at the anvil position of a cubic press and is applied with high temperature and high pressure. The high-temperature high-pressure process flow comprises the following steps: firstly, increasing the pressure to 5.5GPa within 10min, then increasing the temperature to 1100 ℃ at the heating rate of 100 ℃/min, and keeping the temperature for 10min under the target pressure and temperature; and then continuously heating to 1450 ℃, keeping the temperature and the pressure for 40min, synchronously reducing the temperature and the pressure to 60 ℃ and atmospheric environment pressure, stopping the machine, taking out the assembly to obtain a polycrystalline diamond blank, and polishing to obtain the polycrystalline diamond with a compact structure.
Example 5
(1) 20g of bonding agent, namely, according to the molar ratio of Ti to Si to nano-diamond being 3:1:5 (wherein the mass ratio of the nano-diamond particle size is 20% of 2-12 nm, and the particle size is 80% of 100 nm), 80g of micro-diamond (wherein the particle size is 10 microns 40g, 6 microns 25g, 3 microns 10g, and 0.5 microns 5 g); firstly, mixing weighed titanium powder, silicon powder and nano-diamond, filling the mixture into a ball milling tank under the argon condition of a glove box, and sealing the ball milling tank; taking out and putting into a planetary ball mill, wherein the ball-to-material ratio is 20:1, mechanically mixing at 350r/min for 120min, and carrying out mechanical alloying to prepare a bonding agent; taking down the ball milling tank after stopping the machine, opening the ball milling tank under the argon condition of a glove box, putting the weighed micron diamond, uniformly scraping and stirring the micron diamond and the bonding agent, and mechanically ball milling and mixing the mixture for 20min to prepare a mixture; taking down the ball milling tank after stopping the machine, opening the ball milling tank under the argon condition of the glove box, and taking out the prepared mixture for later use;
(2) taking out the mixture, weighing according to the requirement, filling the mixture into a Ti tube, and plugging two ends of the Ti tube; putting the mixture into a metal die, and prepressing and molding the mixture in a hydraulic press at the pressure of 200MPa and room temperature to prepare a prepressed blank;
(3) the pre-pressing blank is assembled with a pressure transmission medium, a carbon tube for heating, a conductive steel ring, a graphite gasket and the like into an assembly according to a common preparation method of the polycrystalline diamond, and the assembly is placed at the anvil position of a cubic press and is applied with high temperature and high pressure. The high-temperature high-pressure process flow comprises the following steps: firstly, increasing the pressure to 6.5GPa within 10min, then increasing the temperature to 1250 ℃ at the heating rate of 50 ℃/min, and keeping the temperature for 10min under the target pressure and temperature; and then continuously heating to 1500 ℃, keeping the temperature and the pressure for 40min, synchronously reducing the temperature and the pressure to 60 ℃ and atmospheric environment pressure, stopping the machine, taking out the assembly to obtain a polycrystalline diamond blank, and polishing to obtain the polycrystalline diamond with a compact structure.
Example 6
(1) 40g of bonding agent, namely, Ti, Si and nano-diamond in a molar ratio of 3:1:4 (wherein the nano-diamond has a particle size of 2-12 nanometers accounting for 40% by mass and a particle size of 100 nanometers accounting for 60%), and 60g of micro-diamond (wherein the particle size is 10 micrometers and 30g, 6 micrometers and 20g, and 0.5 micrometer and 10 g); firstly, mixing weighed titanium powder, silicon powder and nano-diamond, filling the mixture into a ball milling tank under the argon condition of a glove box, and sealing the ball milling tank; taking out and putting into a planetary ball mill, wherein the ball-to-material ratio is 20:1, mechanically mixing for 120min at 400r/min, and carrying out mechanical alloying to prepare a bonding agent; taking down the ball milling tank after stopping the machine, opening the ball milling tank under the argon condition of a glove box, putting the weighed micron diamond, uniformly scraping and stirring the micron diamond and the bonding agent, and mechanically ball milling and mixing the mixture for 20min to prepare a mixture; taking down the ball milling tank after stopping the machine, opening the ball milling tank under the argon condition of the glove box, and taking out the prepared mixture for later use;
(2) taking out the mixture, weighing according to the requirement, filling the mixture into a Ti tube, and plugging two ends of the Ti tube; putting the mixture into a metal die, and prepressing and molding the mixture in a hydraulic press at the pressure of 200MPa and room temperature to prepare a prepressed blank;
(3) the pre-pressing blank is assembled with a pressure transmission medium, a carbon tube for heating, a conductive steel ring, a graphite gasket and the like into an assembly according to a common preparation method of the polycrystalline diamond, and the assembly is placed at the anvil position of a cubic press and is applied with high temperature and high pressure. The high-temperature high-pressure process flow comprises the following steps: firstly, increasing the pressure to 7GPa within 20min, then increasing the temperature to 1200 ℃ at the temperature increase rate of 100 ℃/min, and keeping the temperature for 10min under the target pressure and temperature; and then continuously heating to 1400 ℃, keeping the temperature and the pressure for 10min, synchronously reducing the temperature and the pressure to 60 ℃ and atmospheric environment pressure, stopping the machine, taking out the assembly to obtain a polycrystalline diamond blank, and polishing to obtain the polycrystalline diamond with a compact structure.
Example 7
(1) 20g of bonding agent, namely, 80g of micro-diamond (the grain diameter is 10 microns and 40g, 6 microns and 25g, 3 microns and 10g, and 0.5 microns and 5g) according to the molar ratio of Ti to Si to the nano-diamond of 3:1:3 (the grain diameter of the nano-diamond is 40% in mass ratio of 2-12 nanometers, and the grain diameter of the nano-diamond is 60% in mass ratio of 100 nanometers); firstly, mixing weighed titanium powder, silicon powder and nano-diamond, filling the mixture into a ball milling tank under the argon condition of a glove box, and sealing the ball milling tank; taking out and putting into a planetary ball mill, mechanically mixing for 120min at the speed of 400r/min, and carrying out mechanical alloying to prepare a bonding agent; taking down the ball milling tank after stopping the machine, opening the ball milling tank under the argon condition of a glove box, putting the weighed micron diamond, uniformly scraping and stirring the micron diamond and the bonding agent, and mechanically ball milling and mixing the mixture for 20min to prepare a mixture; taking down the ball milling tank after stopping the machine, opening the ball milling tank under the argon condition of the glove box, and taking out the prepared mixture for later use;
(2) taking out the mixture, weighing according to the requirement, filling the mixture into a Ti tube, and plugging two ends of the Ti tube; putting the mixture into a metal die, and prepressing and molding the mixture in a hydraulic press at the pressure of 100MPa and room temperature to prepare a prepressed blank;
(3) the pre-pressing blank is assembled with a pressure transmission medium, a carbon tube for heating, a conductive steel ring, a graphite gasket and the like into an assembly according to a common preparation method of the polycrystalline diamond, and the assembly is placed at the anvil position of a cubic press and is applied with high temperature and high pressure. The high-temperature high-pressure process flow comprises the following steps: firstly, increasing the pressure to 6.5GPa within 20min, then increasing the temperature to 1150 ℃ at the temperature increase rate of 50 ℃/min, and keeping the temperature for 10min under the target pressure and temperature; and then continuously heating to 1450 ℃, keeping the temperature and the pressure for 10min, synchronously reducing the temperature and the pressure to 60 ℃ and atmospheric environment pressure, stopping the machine, taking out the assembly to obtain a polycrystalline diamond blank, and polishing to obtain the polycrystalline diamond with a compact structure.
Example 8
(1) 30g of bonding agent, 70g of micron diamond (the grain diameter is 10 microns 32g, 6 microns 20g, 3 microns 15g and 0.5 micron 3g) according to the molar ratio of Ti to Si to C being 3:1: 4; firstly, mixing weighed titanium powder, silicon powder and nano-diamond, filling the mixture into a ball milling tank under the argon condition of a glove box, and sealing the ball milling tank; taking out and putting into a planetary ball mill, wherein the ball-to-material ratio is 20:1, mechanically mixing for 120min at 400r/min, and carrying out mechanical alloying to prepare a bonding agent; taking down the ball milling tank after stopping the machine, opening the ball milling tank under the argon condition of a glove box, putting the weighed micron diamond, uniformly scraping and stirring the micron diamond and the bonding agent, and mechanically ball milling and mixing the mixture for 20min to prepare a mixture; taking down the ball milling tank after stopping the machine, opening the ball milling tank under the argon condition of the glove box, and taking out the prepared mixture for later use;
(2) taking out the mixture, weighing according to the requirement, filling the mixture into a Ti tube, and plugging two ends of the Ti tube; putting the mixture into a metal die, and prepressing and molding the mixture in a hydraulic press at the pressure of 200MPa and room temperature to prepare a prepressed blank;
(3) the pre-pressing blank is assembled with a pressure transmission medium, a carbon tube for heating, a conductive steel ring, a graphite gasket and the like into an assembly according to a common preparation method of the polycrystalline diamond, and the assembly is placed at the anvil position of a cubic press and is applied with high temperature and high pressure. The high-temperature high-pressure process flow comprises the following steps: firstly, increasing the pressure to 6.5GPa within 10min, then increasing the temperature to 1150 ℃ at the temperature increase rate of 30 ℃/min, and keeping the temperature for 10min under the target pressure and temperature; and then continuously heating to 1350 ℃, keeping the temperature and the pressure for 20min, synchronously reducing the temperature and the pressure to 60 ℃ and atmospheric environment pressure, stopping the machine, taking out the assembly to obtain a polycrystalline diamond blank, and polishing to obtain the polycrystalline diamond with a compact structure.
Example 9
(1) 20g of bonding agent, namely, according to the molar ratio of Ti to Si to nano-diamond being 3:1:5 (wherein the mass ratio of the nano-diamond particle size is 20% of 2-12 nm, and the particle size is 80% of 100 nm), 80g of micro-diamond (wherein the particle size is 10 microns 40g, 6 microns 25g, 3 microns 10g, and 0.5 microns 5 g); firstly, mixing weighed titanium powder, silicon powder and nano-diamond, filling the mixture into a ball milling tank under the argon condition of a glove box, and sealing the ball milling tank; taking out and putting into a planetary ball mill, wherein the ball-to-material ratio is 20:1, mechanically mixing for 120min at 400r/min, and carrying out mechanical alloying to prepare a bonding agent; taking down the ball milling tank after stopping the machine, opening the ball milling tank under the argon condition of a glove box, putting the weighed micron diamond, uniformly scraping and stirring the micron diamond and the bonding agent, and mechanically ball milling and mixing the mixture for 20min to prepare a mixture; taking down the ball milling tank after stopping the machine, opening the ball milling tank under the argon condition of the glove box, and taking out the prepared mixture for later use;
(2) taking out the mixture, weighing according to the requirement, filling the mixture into a Ti tube, and plugging two ends of the Ti tube; putting the mixture into a metal die, and prepressing and molding the mixture in a hydraulic press at the pressure of 200MPa and room temperature to prepare a prepressed blank;
(3) the pre-pressing blank is assembled with a pressure transmission medium, a carbon tube for heating, a conductive steel ring, a graphite gasket and the like into an assembly according to a common preparation method of the polycrystalline diamond, and the assembly is placed at the anvil position of a cubic press and is applied with high temperature and high pressure. The high-temperature high-pressure process flow comprises the following steps: firstly, increasing the pressure to 6.5GPa within 10min, then increasing the temperature to 1250 ℃ at the heating rate of 50 ℃/min, and keeping the temperature for 10min under the target pressure and temperature; and then continuously heating to 1450 ℃, keeping the temperature and the pressure for 40min, synchronously reducing the temperature and the pressure to 60 ℃ and atmospheric environment pressure, stopping the machine, taking out the assembly to obtain a polycrystalline diamond blank, and polishing to obtain the polycrystalline diamond with a compact structure.
Example 10
(1) 30g of bonding agent, namely, 70g of micro-diamond (the grain diameter is 10 microns 32g, 6 microns 20g, 3 microns 15g and 0.5 micron 3g) according to the molar ratio of Ti to Si to the nano-diamond of 3:1:4 (the grain diameter of the nano-diamond is 20% by mass and the grain diameter is 100 nanometers is 80%); firstly, mixing weighed titanium powder, silicon powder and nano-diamond, filling the mixture into a ball milling tank under the argon condition of a glove box, and sealing the ball milling tank; taking out and putting into a planetary ball mill with a ball-to-material ratio of 20:1, mechanically mixing for 120min at a speed of 450r/min, and carrying out mechanical alloying to prepare a bonding agent; taking down the ball milling tank after stopping the machine, opening the ball milling tank under the argon condition of a glove box, putting the weighed micron diamond, uniformly scraping and stirring the micron diamond and the bonding agent, and mechanically ball milling and mixing the mixture for 20min to prepare a mixture; taking down the ball milling tank after stopping the machine, opening the ball milling tank under the argon condition of the glove box, and taking out the prepared mixture for later use;
(2) taking out the mixture, weighing according to the requirement, filling the mixture into a Ti tube, and plugging two ends of the Ti tube; putting the mixture into a metal die, and prepressing and molding the mixture in a hydraulic press at the pressure of 200MPa and room temperature to prepare a prepressed blank;
(3) the pre-pressing blank is assembled with a pressure transmission medium, a carbon tube for heating, a conductive steel ring, a graphite gasket and the like into an assembly according to a common preparation method of the polycrystalline diamond, and the assembly is placed at the anvil position of a cubic press and is applied with high temperature and high pressure. The high-temperature high-pressure process flow comprises the following steps: firstly, increasing the pressure to 6.0GPa within 10min, then increasing the temperature to 1150 ℃ at the temperature increase rate of 30 ℃/min, and keeping the temperature for 10min under the target pressure and temperature; and then continuously heating to 1500 ℃, keeping the temperature and the pressure for 10min, synchronously reducing the temperature and the pressure to 60 ℃ and atmospheric environment pressure, stopping the machine, taking out the assembly to obtain a polycrystalline diamond blank, and polishing to obtain the polycrystalline diamond with a compact structure.
And (3) testing the structure:
1. the polycrystalline diamond prepared in example 5 was observed by a scanning electron microscope, and the result is shown in fig. 1. The large white particles in fig. 1 are micro-diamonds, and the area in the ring is a shelf area, and as can be seen from fig. 1, the shelf area is filled with a large amount of nano-diamonds.
Fig. 2 is a partially enlarged view of fig. 1, in which the filling of the nano-diamond into the shelf region can be more visually seen.
2. XRD test was performed on the polycrystalline diamonds prepared in example 5, example 9 and example 2, and the results are shown in fig. 3, where 1400 ℃ corresponds to example 2, 1450 ℃ corresponds to example 9 and 1500 ℃ corresponds to example 5 in fig. 3, and it can be seen from fig. 3 that the polycrystalline diamond prepared by the present invention is composed of diamond, TiC, Ti3SiC2And Ti5Si3The phase composition does not remain simple substance Ti and simple substance Si. Since the content of SiC is low, XRD cannot detect it, so that the characteristic peak of SiC is not found in fig. 3.
3. XRD tests were performed on the polycrystalline diamonds prepared in examples 6, 7, 8 and 10, and the results are shown in FIG. 4, 1350 ℃ corresponds to example 8, 1400 ℃ corresponds to example 6, 1450 ℃ corresponds to example 7 and 1500 ℃ corresponds to example 10, and it can be seen from FIG. 4 that the polycrystalline diamonds prepared by the invention are diamond, TiC, SiC and Ti3SiC2And Ti5Si3The compound is composed of pure Ti and pure Si.
The embodiments can know that the invention provides the polycrystalline diamond combined by the compound generated by the in-situ reaction and the preparation method thereof, and solves the problem that the soft spots are left by adding Si, Ti, B, Ni and the like which are easy to remain unreacted Ti, Si and compounds thereof in the 'shed frame region' of the diamond in the traditional PCD preparation method.
The foregoing is only a preferred embodiment of the present invention, and it should be noted that, for those skilled in the art, various modifications and decorations can be made without departing from the principle of the present invention, and these modifications and decorations should also be regarded as the protection scope of the present invention.
Claims (10)
1. A method for preparing compound-bonded polycrystalline diamond by in-situ reaction is characterized by comprising the following steps:
carrying out ball milling on Ti powder, Si powder and nano diamond, and carrying out mechanical alloying to obtain a bonding agent material; the molar ratio of the Ti powder to the Si powder is equal to 3; the molar ratio of the nano diamond to the Si powder is more than 2 and less than or equal to 5;
mixing the bonding agent material with the micron diamond to obtain a mixture;
prepressing the mixture to obtain a prepressing blank;
sintering the pre-pressed blank at high temperature and high pressure to obtain polycrystalline diamond combined with a compound generated by an in-situ reaction;
the high-temperature high-pressure sintering comprises the following steps: sequentially carrying out first high-temperature high-pressure sintering and second high-temperature high-pressure sintering; the temperature of the first high-temperature high-pressure sintering is 1100-1300 ℃, and the heat preservation time is 5-15 min; the temperature of the second high-temperature high-pressure sintering is 1350-1500 ℃, and the heat preservation time is 5-40 min;
the pressure of the first high-temperature high-pressure sintering and the second high-temperature high-pressure sintering is independently more than 5.5 GPa.
2. The method according to claim 1, wherein the particle diameters of the Ti powder and the Si powder are independently 3 to 10 μm.
3. The method according to claim 1, wherein the nanodiamond has a particle size of 2 to 100 nm.
4. The method of claim 1, 2 or 3, wherein the ball milling has a ball to feed ratio of 20: 1; the rotating speed of the ball milling is 350-450 r/min; the ball milling time is more than 120 min.
5. The method according to claim 1, wherein the micro-diamonds have a particle size of 0.5 to 40 μm.
6. The preparation method according to claim 1, wherein the mass content of the binding agent in the mixture is 10-40%.
7. The method according to claim 1, wherein the pre-pressing pressure is 100 to 200 MPa.
8. The production method according to claim 7, wherein the dwell time of the pre-pressing is 10min or more.
9. The polycrystalline diamond prepared by the preparation method of any one of claims 1 to 8, which comprises micro diamond, nano diamond, TiC and Ti3SiC2SiC and TiSi phases.
10. The polycrystalline diamond of claim 9, wherein the TiSi phase comprises TiSi2Phase and/or Ti5Si3And (4) phase(s).
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202110805725.8A CN113528879B (en) | 2021-07-16 | 2021-07-16 | Polycrystalline diamond combined by compounds generated by in-situ reaction and preparation method thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202110805725.8A CN113528879B (en) | 2021-07-16 | 2021-07-16 | Polycrystalline diamond combined by compounds generated by in-situ reaction and preparation method thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN113528879A true CN113528879A (en) | 2021-10-22 |
| CN113528879B CN113528879B (en) | 2022-01-14 |
Family
ID=78128435
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN202110805725.8A Active CN113528879B (en) | 2021-07-16 | 2021-07-16 | Polycrystalline diamond combined by compounds generated by in-situ reaction and preparation method thereof |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN113528879B (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN115433847A (en) * | 2022-09-14 | 2022-12-06 | 河南四方达超硬材料股份有限公司 | Polycrystalline diamond and preparation method thereof, and polycrystalline diamond composite material and preparation method thereof |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101624287A (en) * | 2009-08-07 | 2010-01-13 | 陕西科技大学 | Preparation method for Ti3SiC2 ceramic material |
| CN102114617A (en) * | 2010-12-06 | 2011-07-06 | 中原工学院 | Ti3SiC2-based ceramic bonding agent diamond grinding tool and preparation method thereof |
| GB201311714D0 (en) * | 2013-06-30 | 2013-08-14 | Element Six Abrasives Sa | Superhard constructions & methods of making same |
-
2021
- 2021-07-16 CN CN202110805725.8A patent/CN113528879B/en active Active
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101624287A (en) * | 2009-08-07 | 2010-01-13 | 陕西科技大学 | Preparation method for Ti3SiC2 ceramic material |
| CN102114617A (en) * | 2010-12-06 | 2011-07-06 | 中原工学院 | Ti3SiC2-based ceramic bonding agent diamond grinding tool and preparation method thereof |
| GB201311714D0 (en) * | 2013-06-30 | 2013-08-14 | Element Six Abrasives Sa | Superhard constructions & methods of making same |
Non-Patent Citations (3)
| Title |
|---|
| L. JAWORSKA等: "Preparation of materials based on Ti–Si–C system using high temperature–high pressure method", 《JOURNAL OF MATERIALS PROCESSING TECHNOLOGY》 * |
| XIAOXIN LV等: "Effect of controllable decomposition of MAX phase (Ti3SiC2) on mechanical properties of rapidly sintered polycrystalline diamond by HPHT", 《CERAMIC INTERNATIONAL》 * |
| 刘磊等: "硅钛结合剂聚晶金刚石的制备与性能", 《金刚石与磨料磨具工程》 * |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN115433847A (en) * | 2022-09-14 | 2022-12-06 | 河南四方达超硬材料股份有限公司 | Polycrystalline diamond and preparation method thereof, and polycrystalline diamond composite material and preparation method thereof |
| CN115433847B (en) * | 2022-09-14 | 2024-01-02 | 河南四方达超硬材料股份有限公司 | Polycrystalline diamond and preparation method thereof, polycrystalline diamond composite material and preparation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CN113528879B (en) | 2022-01-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4636253A (en) | Diamond sintered body for tools and method of manufacturing same | |
| KR101123490B1 (en) | Composite sintered compact and cutting tool | |
| CN110257681B (en) | Polycrystalline cubic boron nitride composite sheet and preparation method thereof | |
| WO2009061265A1 (en) | A diamond metal composite | |
| JP5371740B2 (en) | Method for producing cubic boron nitride molded body | |
| CN112063905B (en) | High-performance WC-WCoB-Co complex phase hard alloy and preparation method thereof | |
| CN111266573B (en) | Preparation method of polycrystalline cubic boron nitride composite sheet | |
| CN113528879B (en) | Polycrystalline diamond combined by compounds generated by in-situ reaction and preparation method thereof | |
| JP2023052561A (en) | Tungsten tetraboride composite matrix and uses thereof | |
| CN103305712A (en) | Production method of titanium carbide-based hard alloy | |
| JPH05209248A (en) | High hardness and wear-resistant material | |
| CN110606745A (en) | Metal-free binder phase tungsten carbide hard alloy composite material and preparation method thereof | |
| CN112239360A (en) | Boron oxide, magnesium oxide and reaction product thereof synergistically toughened tungsten carbide composite material and preparation thereof | |
| JPS6137221B2 (en) | ||
| JPS62105911A (en) | Hard diamond mass and production thereof | |
| JPH0215515B2 (en) | ||
| CN114728853B (en) | Polycrystalline diamond with iron-containing binder | |
| CN115233023B (en) | Method for preparing hard alloy and hard alloy | |
| CN111974310B (en) | Method for preparing polycrystalline diamond compact from cobalt catalyst-loaded diamond micro powder | |
| JPS6146540B2 (en) | ||
| CN115108834A (en) | Tungsten carbide sintered body and preparation method thereof | |
| KR820000877B1 (en) | Sintered compact composition for machining tool | |
| CN114901613A (en) | Polycrystalline cubic boron nitride material | |
| JPH0154302B2 (en) | ||
| CN114471365A (en) | Boron-doped nano polycrystalline diamond taking nano graphite as carbon source and preparation method thereof |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| GR01 | Patent grant | ||
| GR01 | Patent grant |